Virno M, Gazzaniga A, Taverniti L, Pecori Giraldi J, De Gregorio F
Department of Ocular Physio-Pharmacology, University of Rome La Sapienza, Italy.
Int Ophthalmol. 1992 Sep;16(4-5):349-53. doi: 10.1007/BF00917989.
The study refers to the clinical experiences performed with several D1 and D2 dopaminergic receptors agonists in 20 patients with high tension open angle glaucoma. The substances were administered topically as eye drops as well as an ocular eye bath. The parameter examined was intraocular pressure (IOP). The substances taken in consideration were: Dopamine, Ibopamine (dopamine analog), Fenoldopam and 3B90 (D1-receptor agonists) and Bromocriptine (dopaminergic agonist with higher affinity for D2 than for D1-receptors). It has been shown that all selective D1-receptors agonists induce a significant increase in IOP only in eyes with hydrodynamic disorders (p < 0.001). Such hypertensive effects could not be antagonized either by topically administered dopaminergic antagonists (Sulpiride, D2-receptors antagonist, and Haloperidol, non-selective dopaminergic antagonist) or by the pretreatment with the commonly used topical antiglaucomatous drugs. The only substance which proved able to inhibit the IOP increase induced by the D1-receptors agonists was the D1-selective antagonist SCH-23390, suggesting that IOP increase may be a result of a stimulation of the D1-receptors. The authors hypothesize that dopaminergic system may play a role in the regulation of aqueous humor hydrodynamics.
该研究涉及对20例高眼压开角型青光眼患者使用几种D1和D2多巴胺能受体激动剂的临床经验。这些物质以眼药水以及眼部浴液的形式局部给药。所检测的参数是眼压(IOP)。所考虑的物质有:多巴胺、异波帕胺(多巴胺类似物)、非诺多泮和3B90(D1受体激动剂)以及溴隐亭(对D2受体的亲和力高于对D1受体的多巴胺能激动剂)。结果表明,所有选择性D1受体激动剂仅在存在流体动力学紊乱的眼睛中引起眼压显著升高(p<0.001)。这种高血压效应既不能被局部给予的多巴胺能拮抗剂(舒必利,D2受体拮抗剂,以及氟哌啶醇,非选择性多巴胺能拮抗剂)所拮抗,也不能被常用的局部抗青光眼药物预处理所拮抗。唯一被证明能够抑制D1受体激动剂引起的眼压升高的物质是D1选择性拮抗剂SCH-23390,这表明眼压升高可能是D1受体受刺激的结果。作者推测多巴胺能系统可能在房水流体动力学调节中起作用。